Canonical Allele Identifier: CA2275255187

Gene: USH1G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74919635T= , CM000679.2:g.74919635T=	GRCh38
NC_000017.10:g.72915730T= , CM000679.1:g.72915730T=	GRCh37
NC_000017.9:g.70427325T=	NCBI36
NG_007882.1:g.8622A=
NG_033062.1:g.361T=
NG_007882.2:g.8629A=
NG_033062.2:g.361T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.1201A= MANE Select	ENSP00000480279.1:p.Met401=
ENST00000579243.1:c.*800A=	ENSP00000462568.1:n.*800A=
ENST00000614341.4:c.1201A=	ENSP00000480279.1:p.Met401=
NM_001282489.2:c.892A=	NP_001269418.1:p.Met298=
NM_173477.4:c.1201A=	NP_775748.2:p.Met401=
XM_011524296.1:c.892A=	XP_011522598.1:p.Met298=
XM_011524296.2:c.892A=	XP_011522598.1:p.Met298=
NM_173477.5:c.1201A= MANE Select	NP_775748.2:p.Met401=
NM_001282489.3:c.892A=	NP_001269418.1:p.Met298=